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首页> 外文期刊>Letters in drug design & discovery >Design, synthesis and evaluation of arylidene pyrrolo and pyrido fused quinazolones as antimicrobial agents
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Design, synthesis and evaluation of arylidene pyrrolo and pyrido fused quinazolones as antimicrobial agents

机译:亚芳基吡咯烷酮和吡啶基稠合喹唑酮类抗菌剂的设计,合成和评价

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摘要

Keeping in view the potential of heterocyclic fused quinazolones and arylidene linked heterocycles , hybrid molecules of these functionalities were designed and synthesised. All the synthesised molecules were characterized by spectroscopic techniques and evaluated for antimicrobial activity against 2 Gram positive bacterial strains; Staphylococcus aureus (MTCC 96) and Bacillus subtilis (MTCC 2451), 3 Gram negative bacterial strains; Escherichia coli (MTCC 82), Pseudomonas aeruginosa (MTCC 2642) and Salmonella typhimurium (MTCC 1251) and 2 fungal strains; Saccharomyces cerevisiae (MTCC 2799) and Candida albicans (MTCC 3018). Among the synthesised molecules, arylidene pyrrolo fused quinazolones displayed significant antimicrobial activity in comparison to arylidene pyrido fused quinazolones. The influence of the electronic factors linked with the arylidene ring was also observed on the antimicrobial potential. Thus the present study highlights the potential of such hybrid molecules as a new class of antimicrobials.
机译:考虑到杂环稠合的喹唑酮和亚芳基连接的杂环的潜力,设计并合成了具有这些功能的杂化分子。所有合成的分子都通过光谱技术进行了表征,并评估了其对2革兰氏阳性细菌菌株的抗菌活性。 3株革兰氏阴性细菌金黄色葡萄球菌(MTCC 96)和枯草芽孢杆菌(MTCC 2451);大肠杆菌(MTCC 82),铜绿假单胞菌(MTCC 2642)和鼠伤寒沙门氏菌(MTCC 1251)和2种真菌菌株;酿酒酵母(MTCC 2799)和白色念珠菌(MTCC 3018)。在合成的分子中,与亚芳基吡咯基稠合的喹唑酮相比,亚芳基吡咯基稠合的喹唑酮显示出显着的抗菌活性。还观察到了与亚芳基环相关的电子因子对抗菌潜能的影响。因此,本研究强调了这种杂合分子作为一类新型抗菌剂的潜力。

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